ENST00000269980.7:c.189T>C
MANE Select
|
ENSP00000269980.2:p.Asp63=
|
|
ENST00000269980.6:c.189T>C
|
ENSP00000269980.2:p.Asp63=
|
|
ENST00000457836.6:c.123T>C
|
ENSP00000416000.2:p.Asp41=
|
|
ENST00000538423.5:n.209T>C
|
|
|
ENST00000540732.3:c.291T>C
|
ENSP00000443246.1:p.Asp97=
|
|
ENST00000542943.5:c.189T>C
|
ENSP00000440345.1:p.Asp63=
|
|
ENST00000595085.5:c.189T>C
|
ENSP00000471150.2:p.Asp63=
|
|
ENST00000604424.1:n.431T>C
|
|
|
NM_000709.3:c.189T>C
|
NP_000700.1:p.Asp63=
|
|
NM_001164783.1:c.189T>C
|
NP_001158255.1:p.Asp63=
|
|
NM_000709.4:c.189T>C
MANE Select
|
NP_000700.1:p.Asp63=
|
|
NM_001164783.2:c.189T>C
|
NP_001158255.1:p.Asp63=
|
|